rs769449, APOE

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.800 1.000 4 2012 2019
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.800 1.000 2 2008 2019
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.710 1.000 1 2014 2014
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 2 2013 2019
High density lipoprotein measurement
1440 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 2 2018 2019
Low density lipoprotein cholesterol measurement
1142 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 2 2018 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 2 2018 2019
Memory performance
CUI: C1285654
Disease: Memory performance
71 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 1 2012 2012
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.700 1.000 1 2012 2012
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.010 1.000 1 2014 2014